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Clinical Operation Scientist Jobs (NOW HIRING)

SanegeneBio Inc.

PM, Clinical Operation

China, TX · On-site

S. and China, we foster a culture of scientific rigor, collaboration, operational excellence, and continuous innovation. We are seeking an experienced Clinical Operations professional to support the ...

Syneos Health, Inc.

Syneos Health ® is a leading fully-integrated life sciences services organization built to ... Summary Roles within Clinical Operations are responsible for ensuring safe and effective operations ...

Clinovo

Sr Clinical Scientist

Cambridge, MA · On-site

Partner with Clinical Operations and Medical Monitoring to support site selection, investigator ... Regulatory & Scientific Contributions * Contribute to clinical sections of regulatory documents ...

Novocure Inc

Clinical Research Scientist

Portsmouth, NH · On-site

$125K - $185K/yr

Working at the intersection of science and operations, you'll collaborate with cross-functional teams across Clinical Development, Clinical Operations, Medical Affairs, Data Management, Regulatory ...

Whoop

Staff Clinical Scientist

Boston, MA · On-site

Translate ambiguous or novel product and clinical questions into rigorous research approaches, recommending study designs that balance scientific rigor, operational feasibility, regulatory ...

Whoop

Staff Clinical Scientist

Boston, MA · On-site

Translate ambiguous or novel product and clinical questions into rigorous research approaches, recommending study designs that balance scientific rigor, operational feasibility, regulatory ...

BALT Group

Clinical Scientist

Irvine, CA · On-site

About this opportunity - Clinical Scientist Description The Clinical Scientist - Medical Writer has a strong background in clinical science and experience in clinical evidence and clinical operations ...

BALT Group

Clinical Scientist

Irvine, CA · On-site

About this opportunity - Clinical Scientist Description The Clinical Scientist - Medical Writer has a strong background in clinical science and experience in clinical evidence and clinical operations ...

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Clinical Operation Scientist information

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How much do clinical operation scientist jobs pay per year?

As of Sep 11, 2026, the average yearly pay for clinical operation scientist in the United States is $94,420.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,000.00 and $119,000.00 per year, depending on experience, location, and employer.

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PM, Clinical Operation

China, TX • On-site

SanegeneBio Inc.
See more jobs at SanegeneBio Inc.external

Other

Posted 9 days ago

Job description

SanegeneBio is a global, venture-backed, clinical-stage biotech company advancing best-in-class genetic medicines. Powered by our proprietary LEAD™ siRNA delivery and chemistry platform, we are developing innovative RNAi therapeutics for cardiometabolic and autoimmune diseases. With R&D operations across the U.S. and China, we foster a culture of scientific rigor, collaboration, operational excellence, and continuous innovation.

We are seeking an experienced Clinical Operations professional to support the execution of global clinical trials. The role is responsible for driving study delivery through cross-functional coordination, vendor management, and operational oversight from start-up to close-out, ensuring high-quality, timely, and compliant execution.

Key Responsibilities
  • Manage clinical trial projects in China and overseas, including monitoring study progress, quality, and budget execution.
  • Participate in the development of overall clinical development plans and clinical trial protocols.
  • Lead the selection and evaluation of clinical trial sites, CROs, SMOs, and other service providers.
  • Draft, review, and finalize key clinical trial documents, including study protocols, source documents, CRFs, clinical trial operation manuals, laboratory manuals, and clinical study reports.
  • Develop project management plans in accordance with study protocols, including team allocation and budget planning, and update these plans as the project progresses.
  • Establish and maintain effective collaboration with investigators, clinical sites, CROs, SMOs, and other vendors to ensure smooth study execution.
  • Communicate and coordinate effectively with cross-functional stakeholders as needed, including medical writing, data management, and biostatistics teams.
  • Provide regular updates on study progress and prepare project status reports.
  • Support quality oversight and management of clinical trial execution, including co-monitoring activities at key sites when necessary, ensuring compliance with protocols, SOPs, and applicable regulations.
  • Coordinate internal audits and quality assurance activities related to clinical trial projects.
  • Participate in regulatory submissions and other R&D-related project activities as required.
Qualifications
  • Background in biochemistry, medicine, or related life science disciplines, with more than 6 years of clinical trial operations and project management experience.
  • Strong professional writing skills, including formal and regulatory documentation.
  • Proficient in English communication, reading, and writing.
  • Excellent time management, communication, coordination, and problem-solving skills./li>
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